Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2

Three loci have been implicated in familial Wilms tumour: WT1 located on chromosome 11p13, FWT1 on 17q12-q21, and FWT2 on 19q13. Two out of 19 Wilms tumour families evaluated showed strong evidence against linkage at all three loci. Both of these families contained at least three cases of Wilms tumo...

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Main Authors: Rapley, E A, Barfoot, R, Bonaïti-Pellié, C, Chompret, A, Foulkes, W, Perusinghe, N, Reeve, A, Royer-Pokora, B, Schumacher, V, Shelling, A, Skeen, J, Tourreil, S de, Weirich, A, Pritchard-Jones, K, Stratton, M R, Rahman, N
Formáid: Artigo
Teanga:Inglês
Foilsithe: Nature Publishing Group 2000
Ábhair:
Regular Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2363495/
https://ncbi.nlm.nih.gov/pubmed/10901367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.2000.1283
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